FDA UDI Not in Commercial Distribution 🇺🇸 United States

Axon

DI: 10705034798608 · Model: 690.053.11 · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Axon
Primary DI
10705034798608
Version / Model
690.053.11
Catalog Number
69005311
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
9
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
f04200db-5476-4e65-b61e-4316b0d2c46d
Distribution End Date
2019-06-20

Device Description

LID FOR AXON(TM) GRAPHIC CASE

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Secondary H981690053110
Primary 10705034798608

Customer Contacts